Priming method

ABSTRACT

The priming method includes the steps of: in a state where a contrast agent bag containing a contrast agent is coupled to a second tube moving a second piston in a second syringe backward to introduce the contrast agent to the second syringe, and with a first tube kept open, moving the second piston in the second syringe forward to discharge air in the second syringe to the outside and to fill the first tube with contrast agent.

TECHNICAL FIELD

The present invention relates to an injector head for introducing contrast agent or other chemical to a patient and, more specifically, to a method of priming for the injector head with rotation mechanism having a mechanism allowing rotation of the injector head in a prescribed direction.

BACKGROUND ART

In a cardiac catheter test, a contrast agent is introduced to a patient using an injector head, and the test is done while imaging the affected part. Utilizing a coronary angiography of providing images of cardiac blood vessels, an operation of blood vessel is performed for widening a narrowed lesion by catheter method. Utilizing left ventricular angiogram imaging the left ventricle of the heart, behavior of cardiac muscle around the left ventricle is tested, by monitoring systole and diastole states of the heart.

Examples of such an injector head are disclosed, for example, in Japanese Patent Laying-Open Nos. 10-165396 (PTD 1) and 10-244002 (PTD 2).

When a test is to be conducted using an injector head, an operation referred to as “priming” is required, for expelling air from a syringe attached to the injector head in advance.

At the time of priming, in order to efficiently expel air from the syringe, it is necessary to have the injector head assume an upward facing orientation (priming orientation), so that a through hole provided at the front end of the syringe faces upward.

On the other hand, when introducing a contrast agent to the patient, the injector head must be rotated broadly to have the injector head in a downward facing orientation (contrast agent injectable orientation), so that the through hole provided at the front end of the syringe faces downward.

To the through hole provided at the front end of the syringe, a tube leading to the patient is coupled. When an operator selects the priming orientation or the contrast agent injectable orientation of the injector head, the injector head is rotated broadly with the tube kept coupled to the through hole of the injector head.

If the injector head is rotated broadly, the tube coupled to the through hole of the syringe also swings significantly. Therefore, the tube must have a margin in its length. If the tube is adapted to have an enough margin in length, the engineer or operator must be very careful to avoid any contact between the tube and other devices. In order to avoid contact between the tube and other devices, arrangement of devices must also be taken care of.

CITATION LIST Patent Document

-   PTD 1: Japanese Patent Laying-Open No. 10-165396 -   PTD 2: Japanese Patent Laying-Open No. 10-244002

SUMMARY OF INVENTION Technical Problem

The problem to be solved by the present invention is that when the injector head is moved between the “priming orientation” and the “contrast agent injectable orientation,” the priming operation must be done with high efficiency.

The present invention was made to solve the above-described problem, and its object is to provide a priming method enabling highly efficient priming operation when the injector head is set to the “priming orientation.”

Solution to Problem

In the priming method based on the present invention, an injector head including a first plunger adapted to be movable forward and backward and a second plunger adapted to be movable forward and backward is used.

The injector head is provided with a first syringe including a first piston detachably coupled to the first plunger and a second syringe including a second piston detachably coupled to the second plunger.

The first syringe has a first through hole provided at a front end side, the second syringe has a second through hole provided at a front end side, and in a state where a first tube is coupled to the first through hole and a second tube is coupled to the second through hole, the priming method is conducted when a contrast agent is introduced to the first syringe and a contrast agent is introduced to the second syringe by the injector head.

A first T-shaped tube is coupled to the other end of the first tube, and the first T-shaped tube is coupled to one end of each of third and fifth tubes. A second T-shaped tube is coupled to the other end of the second tube, and the second T-shaped tube is coupled to one end of each of fourth and sixth tubes.

A third T-shaped tube is coupled to the other end of each of the third and fourth tubes, and to the third T-shaped tube, a seventh tube having the other end coupled to a bag of the contrast agent is coupled. A fourth T-shaped tube is coupled to the other end of each of the fifth and sixth tubes, and to the fourth T-shaped tube, a coupling tube 12 having the other end coupled to a connector is coupled.

A first flow path switching mechanism for switching opening/closing of the third and fifth tubes arranged parallel to each other, and a second flow path switching mechanism for switching opening/closing of the fourth and sixth tubes arranged parallel to each other are provided.

The first flow path switching mechanism has a first change-over valve element arranged between the third and fifth tubes and movable in a direction intersecting a direction of extension of the third and fifth tubes.

The first flow path switching mechanism has a first fixed valve element at a position opposite to the first change-over valve element with the third tube interposed, and a second fixed valve element at a position opposite to the first change-over valve element with the fifth tube interposed.

The second flow path switching mechanism has a second change-over valve element arranged between the fourth and sixth tubes and movable in a direction intersecting a direction of extension of the fourth and sixth tubes.

The second flow path switching mechanism has a third fixed valve element at a position opposite to the second change-over valve element with the fourth tube interposed, and a fourth fixed valve element at a position opposite to the second change-over valve element with the sixth tube interposed.

The priming method includes the following steps:

a first step of tilting the injector head and thereby tilting the first and second syringes to have the first through hole positioned upper than the first piston and the second through hole positioned upper than the second piston;

a second step, following the first step, of moving the first change-over valve element to the side of the first fixed valve element to close the third tube and moving the second change-over valve element to the side of the third fixed valve element to close the fourth tube and, in this state, moving the first piston in the first syringe to the foremost position to discharge air in the first syringe to the outside and moving the second piston in the second syringe to the foremost position to discharge air in the second syringe to the outside;

a third step, following the second step, of moving the second change-over valve element of the second flow path switching mechanism to the side of the fourth fixed valve element to open the fourth tube and to close the sixth tube and, in this state, with a contrast agent bag containing the contrast agent coupled to the second tube, moving the second piston in the second syringe backward to introduce a prescribed amount of contrast agent from the contrast agent bag to the second syringe;

a fourth step, following the third step, of moving the second change-over valve element to the side of the third fixed valve element to close the fourth tube and moving the first change-over valve element to the side of the second fixed valve element to close the fifth tube and, in this state, moving the second piston in the second syringe backward to introduce a prescribed amount of air to the second syringe;

a fifth step, following the fourth step, of moving the first change-over valve element to the side of the first fixed valve element to close the third tube and, in this state, moving the second piston in the second syringe forward to discharge air in the second syringe to the outside and filling the second tube with the contrast agent;

a sixth step, following the fifth step, of moving the first change-over valve element of the first flow path switching mechanism to the side of the second fixed valve element to open the third tube and to close the fifth tube and, in this state, moving the first piston in the first syringe backward to introduce a prescribed amount of contrast agent from the contrast agent bag to the first syringe;

a seventh step, following the sixth step, of moving the first change-over valve element to the side of the first fixed valve element to close the third tube and, in this state, moving the second piston in the second syringe backward to introduce a prescribed amount of air to the second syringe; and

an eighth step, following the seventh step, of moving the second change-over valve element to the side of the fourth fixed valve element to close the sixth tube, and in this state, moving the second piston in the second syringe backward to introduce the contrast agent to the second syringe and, with the first tube being kept open, moving the second piston in the second syringe forward to discharge air in the second syringe to the outside and filling the first tube with the contrast agent.

According to another aspect, the coupling tube is further provided with a first air sensor for detecting entrance of air to the coupling tube; the seventh tube is further provided with a second air sensor for detecting entrance of air to the seventh tube; at the fifth step, the second piston in the second syringe is moved forward until passage of the contrast agent is detected by the first air sensor, and at the eighth step, the first piston in the first syringe is moved forward until passage of the contrast agent is detected by the first air sensor, and the second piston in the second syringe is moved backward until passage of the contrast agent is no longer detected by the second air sensor.

According to a further aspect, the injector head includes: a supporting part; a rotating part fixed on the supporting part to have a rotation axis extending substantially horizontally; an injector head body fixed on the rotating part to be rotatable about the rotation axis; and a syringe detachably attached to the injector head body.

In a state where the first and second syringes are attached to the injector head body, when viewed from the direction perpendicular to and parallel to the rotation axis, central axis line of the first and second syringes is inclined with respect to the rotation axis.

By rotating the injector head body about the rotation axis as the center of rotation, selection is possible between a state in which the first and second syringes assume a priming orientation with the first through hole side of the first syringe and the second through hole side of the second syringe positioned upper than the injector head body and a state in which the first through hole of the first syringe assumes a contrast agent injectable orientation with the first through hole side of the first syringe and the second through hole of the second syringe positioned lower.

The first through hole is provided at a position eccentric to the central axis line of the first syringe; the second through hole is provided at a position eccentric to the central axis line of the second syringe; the first and second syringes are attached to the injector head body such that when the first and second syringes are in the priming orientation, the first and second through holes are positioned at the uppermost positions.

Advantageous Effects of Invention

By the priming method of the present invention, a priming method that enables highly efficient priming operation when the injector head is set to the “priming orientation” can be provided.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 is a side view showing the injector head with rotation mechanism (in priming orientation) in accordance with an embodiment.

FIG. 2 is a view from a direction of an arrow II of FIG. 1.

FIG. 3 is a side view showing the injector head with rotation mechanism (in contrast agent injectable orientation) in accordance with an embodiment.

FIG. 4 is a view from a direction of an arrow IV of FIG. 3.

FIG. 5 is a side view from a direction of an arrow V of FIG. 6, of the syringe attached to the injector head with rotation mechanism in accordance with an embodiment.

FIG. 6 is a cross-sectional view taken along the line VI-VI of FIG. 5, of the syringe attached to the injector head with rotation mechanism in accordance with an embodiment.

FIG. 7 shows a contrast agent introducing line to a patient, using the injector head with rotation mechanism in accordance with an embodiment.

FIG. 8 shows a first step of the priming process for the injector head with rotation mechanism in accordance with an embodiment.

FIG. 9 shows a second step of the priming process for the injector head with rotation mechanism in accordance with an embodiment.

FIG. 10 shows a third step of the priming process for the injector head with rotation mechanism in accordance with an embodiment.

FIG. 11 shows a fourth step of the priming process for the injector head with rotation mechanism in accordance with an embodiment.

FIG. 12 shows a fifth step of the priming process for the injector head with rotation mechanism in accordance with an embodiment.

FIG. 13 shows a sixth step of the priming process for the injector head with rotation mechanism in accordance with an embodiment.

FIG. 14 shows a seventh step of the priming process for the injector head with rotation mechanism in accordance with an embodiment.

FIG. 15 shows an eighth step of the priming process for the injector head with rotation mechanism in accordance with an embodiment.

FIG. 16 is a first illustration showing the process of contrast agent injection and suction by the injector head with rotation mechanism in accordance with an embodiment.

FIG. 17 is a second illustration showing the process of contrast agent injection and suction by the injector head with rotation mechanism in accordance with an embodiment.

FIG. 18 is a third illustration showing the process of contrast agent injection and suction by the injector head with rotation mechanism in accordance with an embodiment.

FIG. 19 is a plan view showing the state of contrast agent injection to a patient using the injector head with rotation mechanism in accordance with an embodiment.

FIG. 20 shows the injector head with rotation mechanism in accordance with an embodiment, in the priming orientation, viewed from the side of the engineer shown in FIG. 19.

FIG. 21 shows the injector head with rotation mechanism in accordance with an embodiment, in the contrast agent injectable orientation, viewed from the side of the doctor shown in FIG. 19.

FIG. 22 shows a flow path switching device of an alternative example, used in the injector head with rotation mechanism in accordance with an embodiment.

FIG. 23 is a cross-sectional view from a direction of an arrow XXIII of FIG. 22.

FIG. 24 is a cross-sectional view from a direction of an arrow XXIV of FIG. 22.

FIG. 25 shows an internal structure of a second flow path switching device of the alternative example, used in the injector head with rotation mechanism in accordance with an embodiment.

FIG. 26 is a first illustration showing a state of operation of the second flow path switching device of the alternative example, used in the injector head with rotation mechanism in accordance with an embodiment.

FIG. 27 is a second illustration showing a state of operation of the second flow path switching device of the alternative example, used in the injector head with rotation mechanism in accordance with an embodiment.

FIG. 28 is a third illustration showing a state of operation of the second flow path switching device of the alternative example, used in the injector head with rotation mechanism in accordance with an embodiment.

FIG. 29 is a fourth illustration showing a state of operation of the second flow path switching device of the alternative example, used in the injector head with rotation mechanism in accordance with an embodiment.

FIG. 30 shows a state of attachment of the injector head with rotation mechanism in accordance with another embodiment.

FIG. 31 shows a state of attachment of the injector head with rotation mechanism in accordance with another embodiment.

DESCRIPTION OF EMBODIMENTS

In the following, the injector head with rotation mechanism and the priming method thereof based on the present invention will be described. In the embodiments described below, the same or corresponding components will be denoted by the same reference characters, and description thereof may not be repeated. Any numbers and amounts mentioned are not limiting the scope of the invention, unless specifically described to the contrary.

In the figures, for easier understanding of the contrast agent in the syringe, piston position and plunger position, the syringe is shown in cross-sections. The priming orientation refers to a state for performing a preliminary work (such as filling the syringe with the contrast agent) before injecting the contrast agent, and the contrast agent injectable orientation refers to the orientation ready to start injection of the contrast agent and the orientation during injection of the contrast agent.

(Injector Head 1 with Rotation Mechanism)

Referring to FIGS. 1 to 6, injector head 1 with rotation mechanism in accordance with an embodiment of the present invention will be described. FIG. 1 is a side view showing injector head 1 with rotation mechanism (in priming orientation), FIG. 2 is a view from a direction of an arrow II of FIG. 1. FIG. 3 is a side view showing injector head 1 with rotation mechanism (in contrast agent injectable orientation), and FIG. 4 is a view from a direction of an arrow IV of FIG. 3. FIG. 5 is a side view of a syringe 510 from a direction of an arrow V of FIG. 6, and FIG. 6 is a cross-sectional view taken along the line VI-VI of FIG. 5.

Injector head 1 with rotation mechanism includes: a support post 900 as a supporting part; a rotating part 700 fixed on support post 900 to have its rotation axis AL extending substantially horizontally; an injector head body 100 fixed to rotating part 700 to be rotatable about the rotation axis AL; and first and second syringes 510A and 510B detachably attached to injector head body 100. A roller bearing or the like is used for rotating part 700.

To a through hole 512 formed at the front end portion of each of the first and second syringes 510A and 510B, a first flow path switching device 600 is coupled. Details of the first flow path switching device 600 will be described later. On a side surface of injector head body 100, an operation monitor 110 implemented by a touch-panel is provided (see FIG. 3).

As the first and second syringes 510A and 510B, a syringe having such a shape as shown in FIGS. 5 and 6 is used. The syringe has a cylindrical part 514 having front end side closed and back end opened to receive a piston 511 to be fit in liquid-tight manner, a through hole 512 provided on the front end side, and a flange provided at the back end side.

Piston 511 includes a piston rubber 511 a and a piston core 511 b covered by piston rubber 511 a. To piston core 511 b, a plunger 100P provided inside injector head 100 is coupled. Cylindrical part 514 is fixed on injector head body 100.

As plunger 100P moves forward and backward, piston 511 also moves forward/backward in cylindrical part 514. Piston rubber 511 a moves while maintaining liquid-tightness with respect to the inner circumferential surface of cylindrical part 514.

Syringe 510 in accordance with the present embodiment has a through hole 512 at a position eccentric from the central axis line SL of syringe 510. The central axis line of syringe 510 means a phantom line extending from the front side to the back side passing through the central axis of syringe 510.

Again referring to FIGS. 1 to 4, in the present embodiment, in a state where the first and second syringes 510A and 510B are attached to injector head body 100, when viewed from a direction perpendicular to and parallel to the rotation axis AL (in a direction perpendicular to the drawing sheet), the central axis lines SL of the first and second syringes 510A and 510B are inclined from rotation axis AL.

When viewed from the direction perpendicular to and parallel to the rotation axis AL (in a direction perpendicular to the drawing sheet), the angle (α) at which the central axis line SL and the rotation axis AL intersect is about 5 to about 30 degrees, preferably about 7 to about 25 degrees, and more preferably, about 10 to about 15 degrees.

Specifically, referring to FIG. 1, injector head body 100 has a substantially rectangular parallelepiped shape, the first and second syringes 510A and 510B are attached to a first surface 100 a of injector head body 100, and rotating part 700 is fixed to an area at an upper corner (near the third surface 100 c) of a second surface 100 b opposite to the first surface 100 a. In the shown example, the first and second syringes 510A and 510B are filled with contrast agent Z.

In the priming orientation shown in FIGS. 1 and 2, a third surface 100 c positioned on the upper side between the first and second surfaces 100 a and 100 b is inclined upward from the side of the second surface 100 b to the side of the first surface 100 a, and a fourth surface 100 d positioned on the lower side between the first and second surfaces 100 a and 100 b is also inclined upward from the side of the second surface 100 b to the side of the first surface 100 a.

Further, in the priming orientation, the first and second syringes 510A and 510B are attached to injector head body 100 such that through hole 512 of each of the first and second syringes 510A and 510B is positioned at the uppermost side.

Referring to FIGS. 3 and 4, in the contrast agent injectable orientation with injection head body 100 rotated (in the direction of an arrow RA1 of FIG. 2) about the rotation axis AL as the center of rotation, the fourth surface 100 d positioned on the upper side between the first and second surfaces 100 a and 100 b is inclined downward from the side of the second surface 100 b to the side of the first surface 100 a, and the fourth surface 100 d positioned on the lower side between the first and second surfaces 100 a and 100 b is also inclined downward from the side of the second surface 100 b to the side of the first surface 100 a.

By rotating injector head body 100 about the rotation axis AL as the center of rotation, injector head 1 with rotation mechanism in accordance with the present embodiment can selectively be set to the state (the state shown in FIGS. 1 and 2) in which the first and second syringes 510A and 510B assume the priming orientation with the through holes 512 of the first and second syringes 510 A and 5100B positioned upper than the injector head body 100, and a state (the state shown in FIGS. 3 and 4) in which the first and second syringes 510A and 510B assume the contrast agent injectable orientation with the through holes 512 of the first and second syringes 510A and 510B positioned lower than the injector head body 100.

In the priming orientation shown in FIGS. 1 and 2, when viewed from the direction perpendicular to and parallel to the rotation axis AL, the central axis line SL of the first syringe 510A intersects the rotation axis AL on the side of through hole 512 of the first syringe 510A. In the contrast agent injectable orientation shown in FIGS. 3 and 4, the first syringe 510A is attached to injector head body 100 such that, when viewed from the direction perpendicular to and parallel to the rotation axis AL, the central axis line SL of the first syringe 510A intersects the rotation axis AL on the side of injector head body 100.

In the priming orientation shown in FIGS. 1 and 2, when viewed from the direction perpendicular to and parallel to the rotation axis AL, the central axis line SL of the second syringe 510B intersects the rotation axis AL on the side of injector head body 100 of the second syringe 510R. In the contrast agent injectable orientation shown in FIGS. 3 and 4, the second syringe 510B is attached to injector head body 100 such that, when viewed from the direction perpendicular to and parallel to the rotation axis AL, the central axis line SL of the second syringe 510B intersects the rotation axis AL on the side of through hole 512 of the second syringe 510B.

Consequently, even when injector head body 100 rotates between the “priming orientation” shown in FIGS. 1 and 2 and the “contrast agent injectable orientation” shown in FIGS. 3 and 4, coupling tube 12 extending from first flow path switching device 600 coupled to the first and second syringes 510A and 510B moves only around rotation axis AL.

As a result, interference between coupling tube 12 coupled to injector head 1 with rotation mechanism in accordance with the present embodiment and other devices becomes less likely. Therefore, ample margin for the tube length becomes unnecessary. Further, the burden on the engineer paying attention to avoid contact between the tube and other devices can be alleviated.

Though double-syringe type injector head 1 with rotation mechanism having two syringes has been described, the number of syringes is not limited to two, and the invention is applicable to a single-syringe type injector head with rotation mechanism using either one of the syringes.

Though a syringe having through hole 512 eccentric to central axis line CL is used as syringe 510, a syringe having through hole 512 provided on the central axis line CL may be used.

(Contrast Agent Injection Line L1000)

Next, a contrast agent injection line L1000 to the patient using injector head 1 with rotation mechanism having the structure above will be described with reference to FIG. 7. To the first and second syringes 510A and 510B attached to injector head body 100, first flow path switching device 600 is coupled. Details of first flow path switching device 600 will be described later.

Contrast agent injection line L1000 can be divided to a multi-use section S1 used for a plurality of patients, and one-time use sections S2 and S3 used only for one patient.

The multi-use section S1 will be described. Multi-use section S1 is shown surrounded by dotted lines in the figure. Multi-use section S1 has first flow path switching device 600. To first flow path switching device 600, a seventh tube 15 is coupled, and to the seventh tube 15, a contrast agent bag 16 is coupled. To first flow path switching device 600, coupling tube 12 leading to the patient is coupled. At the tip end of coupling tube 12, a connector 13 is connected.

The one-time use section S2 will be described. One-time use section S2 is shown surrounded by dotted lines in the figure. One-time use section S2 has a main tube 17 having a connector 14 connected to one end and a connector 20 connected to the other end. Connector 14 is connected to connector 13 of coupling tube 12.

Main tube 17 has a branch tube 17 a. At the tip end of branch tube 17 a, a connector 25 is connected. Opening/closing of main tube 17 and branch tube 17 a is controlled by a second flow path switching device 800. Second flow path switching device 800 has fixed valve elements 801 and 802 and a change-over valve element 803, and change-over valve element 803 is controlled to move in the direction of an arrow RA10 in the figure. By fixed valve element 801 and change-over valve element 803, opening/closing of main tube 17 is controlled, and by fixed valve element 802 and change-over valve element 803, opening/closing of branch tube 17 a is controlled.

Connector 25 of branch tube 17 a is coupled to a connector 26 provided on a normal saline tube 19. Normal saline tube 19 has the other end coupled to a saline bag 21. A blood pressure transducer 300, a roller pump 400, and a third air sensor AS3 are provided on normal saline tube 19.

The one-time use section S3 will be described. One-time use section S3 is shown surrounded by dotted lines in the figure. One-time use section S3 has a tube 22 having one end connected to a connector 24 and the other end connected to a connector 23. To connector 24, connector 20 of main tube 17 is coupled. To connector 23, a catheter inserted to a blood vessel of a patient is coupled.

Blood pressure of a patient is measured using normal saline, with main tube 17 closed by fixed valve element 801 and change-over valve element 803 and branch tube 17 a communicated with saline bag 21. For the measurement of blood pressure, electric signals from blood pressure transducer 300 are used.

When contrast agent is to be introduced from injector head 1 with rotation mechanism to the patient, branch tube 17 a is closed and the main tube 17 is opened by fixed valve element 802 and change-over valve element 803.

(First Flow Path Switching Device 600 and Priming Operation)

Next, referring to FIGS. 8 to 15, first flow path switching device 600 and the priming operation will be described. FIGS. 8 to 15 show the first to ninth steps of the priming process in injector head 1 with rotation mechanism. In the present embodiment, the priming operation as described below is automatically executed by a control device mounted inside injector head body 100.

First flow path switching device 600 should be represented by dotted lines as the main components are positioned on the other side of the device. For convenience of description, however, the device is shown by solid lines in FIGS. 8 to 15.

Referring to FIG. 8, in the priming operation, the first and second syringes 510A and 510B are positioned such that through holes 512 face upward, as described with reference to FIGS. 1 and 2.

To injector head body 100, first syringe 510A having contrast agent Z filled therein and second syringe 510B having contrast agent Z filled therein are mounted. A piston 511A coupled to a first plunger 100Pa is provided inside first syringe 510A, and a second piston 511B coupled to a second plunger 100Pb is provided inside second syringe 510B.

One end of a first tube 10A is coupled to the first syringe 510A. The other end of first tube 10A is coupled to a first T-shaped tube 11A. To the first T-shaped tube 11A, one end of a third tube 111A and one end of a fifth tube 112A are coupled, respectively.

One end of a second tube 10B is coupled to the second syringe 510B. The other end of second tube 10B is coupled to a second T-shape tube 11B. To the second T-shaped tube 11B, one end of a fourth tube 111B and one end of a sixth tube 112B are coupled, respectively.

The third and fourth tubes 11A and 111B each have the other end coupled to a third T-shaped tube 11C. Further, to the third T-shaped tube 11C, the seventh tube 15, having the other end coupled to a contrast agent bag 16, is coupled.

The fifth and sixth tubes 112A and 112B each have the other end coupled to a fourth T-shaped tube 11D. To the fourth T-shaped tube 11D, coupling tube 12, having the other end coupled to connector 13, is coupled.

A first air sensor AS1 detecting entrance of air to the tube is provided on coupling tube 12, and a second air sensor AS2 detecting entrance of air to the tube is provided on the seventh tube 15.

(First Flow Path Switching Device 600)

First flow path switching device 600 is provided for switching opening/closing of the third tube 111A and opening/closing of the fifth tube 112A. First flow path switching device 600 has a first flow path switching mechanism 600A and a second flow path switching mechanism 600B.

First flow path switching mechanism 600A is provided for switching between the third and fifth tubes 111A and 112A arranged parallel to each other, and the second flow path switching mechanism 600B is provided for switching between the fourth and sixth tubes 111B and 112B arranged parallel to each other.

The first flow path switching mechanism 600A has a first change-over valve element 603 provided between the third and fifth tubes 111A and 112A and movable in a direction intersecting the direction of extension of the tubes. Further, first flow path switching mechanism 600A has first and second fixed valve elements 601 and 602 at positions opposite to the first change-over valve element 603 with respective tubes interposed.

Similarly, the second flow path switching mechanism 600B has a second change-over valve element 606 provided between the fourth and sixth tubes 111B and 112B and movable in a direction intersecting the direction of extension of the tubes. Further, the second flow path switching mechanism 600B has third and fourth fixed valve elements 604 and 605 at positions opposite to the second change-over valve element 606 with respective tubes interposed.

(Priming Operation: First Step)

Next, the priming operation using the first flow path switching device 600 having the structure above will be described with reference to FIGS. 8 to 15. Injector head 1 with rotation mechanism in accordance with the present embodiment is set to the priming orientation in which the side of first through hole 512A of first syringe 510A is positioned upper than the side of injector head body 100 (first plunger (100Pa)) and the side of second through hole 512B of second syringe 510B is positioned upper than the side of injector head body 100 (second plunger (100Pb)), by rotating injector head body 100 about the rotation axis AL as the center of rotation, as shown in FIGS. 1 and 2. The priming operation refers to the operation of expelling air from the first and second syringes 510A and 510B and from various tubes.

Referring to FIG. 8, in a state where contrast agent bag 16 is not coupled to the seventh tube 15, the first piston 511A in the first syringe 510A and the second piston 511B in the second syringe 510B, not filled with contrast agent but empty, are set to the rearmost positions. Further, the first change-over valve element 603 of the first flow path switching mechanism 600A and the second change-over valve element 606 are positioned at neutral positions, and the third, fifth, fourth and sixth tubes 111A, 112A. 111B and 112B are opened. Here, the first air sensor does not output any signal.

(Second Step)

Next, as shown in FIG. 9, the first change-over valve element 603 of first flow path switching mechanism 600A is moved to the side of the first fixed valve element 601, to close the third tube 111A. Further, the second change-over valve element 606 of the second flow path switching mechanism 600B is moved to the side of the third fixed valve element 604, to close the fourth tube 111B. Next, contrast agent bag 16 is coupled to the seventh tube 15, and the first piston 111A in the first syringe 510A and the second piston 511B in the second syringe 510B are moved to the foremost position (in the direction indicated by an arrow F in FIG. 9), to discharge air in the first and second syringes 510A and 510B to the outside.

(Third Step)

Next, as shown in FIG. 10, the second change-over valve element 606 of the second flow path changing mechanism 600B is moved to the side of the fourth fixed valve element 605, to open the fourth tube 111B and close the sixth tube 112B. Thereafter, the second piston 511B in the second syringe 510B is moved backward (in the direction of the arrow B in the figure), and contrast agent Z is introduced from contrast agent bag 16 to the second syringe 510B.

(Fourth Step)

Next, referring to FIG. 11, after a prescribed amount of contrast agent Z is introduced to the second syringe 510B, the second change-over valve element 606 is moved to the side of the third fixed valve element 604 to close the fourth tube 111B, and the first change-over valve element 603 is moved to the side of the second fixed valve element 602 to close the fifth tube 112A. Thereafter, the second piston 511B in the second syringe 510B is moved backward (in the direction of the arrow B in the figure), to introduce a prescribed amount of air to the second syringe 510B.

(Fifth Step)

Next, referring to FIG. 12, the first change-over valve element 603 is moved to the side of the first fixed valve element 601, to close the third tube 111A. Thereafter, the second piston 511B in the second syringe 510B is moved forward (in the direction of the arrow F in FIG. 12) until passage of the contrast agent is detected by the first air sensor AS1.

(Sixth Step)

Next, referring to FIG. 13, the first change-over valve element 603 of the first flow path changing mechanism 600A is moved to the side of the second fixed valve element 602 to open the third tube 111A and to close the fifth tube 112A. Thereafter, the first piston 511A in the first syringe 510A is moved backward (in the direction of the arrow B in FIG. 13), and the contrast agent Z is introduced from contrast agent bag 16 to the first syringe 510A.

(Seventh Step)

Next, referring to FIG. 14, after a prescribed amount of contrast agent Z is introduced to the first syringe 510A, the first change-over valve element 603 is moved to the side of the first fixed valve element 601 to close the third tube 111A. Thereafter, the first piston 511A in the second syringe 51A is moved backward (in the direction of the arrow B in FIG. 14), to introduce a prescribed amount of air to the first syringe 510A.

(Eighth Step)

Next, referring to FIG. 15, the second change-over valve element 606 is moved to the side of the fourth fixed valve element 605 to close the sixth tube 112B. In this state, the first piston 511A in the first syringe 510A is moved forward (in the direction of the arrow F in FIG. 15) until passage of the contrast agent is detected by the first air sensor AS1 and the second piston 511B in the second syringe 510B is moved backward (in the direction of the arrow B in FIG. 15) until the passage of contrast agent is no longer detected by the second air sensor AS2.

By the operations described above, the priming operation of the first and second syringes 510A and 510B using the first flow path changing device 600 is completed, and air is expelled from the first and second syringes 510A and 510B as well as from the first, second, third, fourth, fifth and sixth tubes 10A, 10B, 111A, 111B, 112A and 112B.

In the priming process described above, presence/absence of the contrast agent Z in the tube is detected by using first and second air sensors AS1 and AS2. If capacity of the syringes, length of each tube, capacity of each tube and the like are known in advance, the priming process may be executed without using the first and second air sensors AS1 and AS2.

(Contrast Agent Injecting Operation)

Next, the operation of injecting contrast agent using the first flow path switching device 600 having the structure as above will be described with reference to FIGS. 16 to 18. After the completion of the above-described priming operation, injector head 1 with rotation mechanism is set to the contrast agent injectable orientation in which the first through hole 512A of the first syringe 510A is positioned lower than injector head body 100 (the first plunger (100Pa)) and the second through hole 512B of the second syringe 510B is positioned lower than injector head body 100 (the second plunger (100Pb)), by rotating injector head body 100 about the rotation axis AL as the center of rotation, as shown in FIGS. 3 and 4.

Referring to FIG. 16, the first change-over valve element 603 of the first flow path switching mechanism 600A is moved to the side of the first fixed valve element 601, to close the third tube 111A. The second change-over valve element 606 of the second flow path switching mechanism 600B is moved to the side of the fourth fixed valve element 605, to close the sixth tube 112B.

Consequently, the first syringe 510A comes to be communicated with coupling tube 12. By the driving of injector head body 100, the first plunger 100Pa is moved forward (in the direction of the arrow F in FIG. 16), and the contrast agent inside is fed through contrast agent injection line L1000 to the patient.

Next, referring to FIG. 17, when the contrast agent in the first syringe 510A is used up, switching between the first and second flow path switching mechanisms 600A and 600B is realized by the first flow path switching device 600. Specifically, the first change-over valve element 603 of the first flow path switching mechanism 600A is moved to the side of the second fixed valve element 602 to close the fifth tube 112A. Further, the second change-over valve element 606 of the second flow path switching mechanism 600B is moved to the side of the third fixed valve element 604 to close the fourth tube 111B.

Consequently, the first syringe 510A is communicated with contrast agent bag 16, and the second syringe 510B is communicated with coupling tube 12. Thus, by simultaneously moving backward the first plunger 100Pa of the first syringe 510A (in the direction of the arrow B in FIG. 17) and moving forward the second plunger 100Pb of the second syringe 510B (in the direction of the arrow F in FIG. 17), suction of contrast agent Z to the first syringe 510A and injection of contrast agent Z from the second syringe 510B can be attained simultaneously. If it is unnecessary to perform the contrast agent suction process to the first syringe 510A, backward movement of the first plunger 100Pa is unnecessary.

By simultaneously moving forward the first plunger 100Pa of the first syringe 510A and moving backward the second plunger 100Pb of the second syringe 510B in the similar manner, it is also possible to simultaneously attain the process of injecting the contrast agent from the first syringe 510A and the contrast agent suction process to the second syringe 510B.

(Mixed Injection)

Referring to FIG. 14, by directly coupling the third tube 111A to the eighth tube 15A coupled to contrast agent bag 16 and directly coupling the fourth tube 111B to the ninth tube 15B coupled to saline bag 21, without using the third T-shaped tube 11C, mixed injection becomes possible.

Specifically, the first change-over valve element 603 of the first flow path switching mechanism 600A is moved to the side of the first fixed valve element 601 to close the third tube 111A. Further, the second change-over valve element 606 of the second flow path switching mechanism 600B is moved to the side of the third fixed valve element 604, to close the fourth tube 111B. Consequently, the first and second syringes 510A and 510B are communicated with coupling tube 12, so that mixed injection of contrast agent Z and normal saline to the patient becomes possible.

Further, by switching the first change-over valve element 603 of the first flow path switching mechanism 600A and the second change-over valve element 606 of the second flow path switching mechanism 600B to close the fifth and fourth tubes 112A and 111B, suction of the contrast agent to first syringe 510A and suction of normal saline to the second syringe 510B can be attained simultaneously.

(Positions of Engineer and Doctor)

Next, positions of the engineer and the doctor when a test is conducted using injector head 1 with rotation mechanism in accordance with the present embodiment will be described with reference to FIGS. 19 to 21. FIG. 19 is a plan view showing the state of contrast agent injection to a patient 2000 using injector head 1 with rotation mechanism, FIG. 20 shows injector head 1 with rotation mechanism in the priming orientation, viewed from the side of the engineer shown in FIG. 19, and FIG. 21 shows injector head 1 with rotation mechanism in the contrast agent injectable orientation, viewed from the side of the doctor shown in FIG. 19.

Referring to FIGS. 19 and 20, the above-described priming operation is carried out by an engineer 3000. Therefore, when injector head 1 with rotation mechanism in accordance with the present embodiment is placed on the left side of a patient 2000 on a bed 1000, it follows that the engineer 3000 also stands on the left side of patient 2000, that is, on the same side of injector head 1 with rotation mechanism.

In injector head body 100, an orientation sensor (not shown) for detecting the orientation is provided, and operation information in accordance with the priming operation is displayed on an operation monitor 110 implemented by a touch-panel.

Referring to FIGS. 19 and 21, the contrast agent injecting operation with injector head 1 with rotation mechanism rotated is carried out by a doctor 4000. Here, it follows that doctor 4000 stands opposite to engineer 3000, on the other side of bed 1000.

Because of the rotation, operation monitor 110 comes to face doctor 4000, and the orientation is detected by the orientation sensor provided inside and the operation instruction in accordance with the contrast agent injecting operation is displayed on operation monitor 110.

In this manner, when injector head 1 with rotation mechanism in accordance with the present embodiment is used, the test can be conducted smooth even when engineer 3000 and doctor 4000 stand on opposite sides of bed 1000.

(Alternative Example of Second Flow Path Switching Device 800A)

Next, an alternative example of the second flow path switching device 800A, corresponding to the second flow path switching device 800 shown in FIG. 7, will be described with reference to FIGS. 22 to 29. FIG. 22 shows the second flow path switching device 800A, FIG. 23 is a cross-sectional view from a direction of an arrow XXIII of FIG. 22, FIG. 24 is a cross-sectional view from a direction of an arrow XXIV of FIG. 22, FIG. 25 shows an internal structure of the second flow path switching device 800A, and FIGS. 26 to 29 are first to fourth illustrations showing state of operations of the second flow path switching device 800A.

Referring to FIGS. 22 to 24, the second flow path switching device 800A has a cover 851. On three of the four side surfaces of cover 851 (left side surface, right side surface and lower side surface in the figure), tube receiving recesses 851 a are provided. Main tube 17 and branch tube 17 a are fixed on tube receiving recesses 851 a.

Referring to FIG. 25, the second flow path switching device 800A has a main body 810. On main body 810, cover 851 with main tube 17 and branch tube 17 a fixed, is detachably attached. It is noted that cover 851 is not shown in FIG. 25.

At upper and lower positions of main body 810, engaging pieces 861 and 862 are provided to detachably hold cover 851, pinching cover 851 both from the upper and lower sides.

At the central position of main body 810, a rotating cam 870 is provided, which rotates about a rotation shaft 870 a as the center of rotation. On the outer circumferential surface of rotating cam 870, a cam face is formed, to control movement of movable valve elements 821 and 822, which will be described later. Rotation of rotating cam 870 is controlled by a driving device (servo motor or the like) provided in main body 810.

A fixed valve element 811 is fixed on main body 810 at an upper side of rotating cam 870. Fixed valve element 811 has a fixed projection 811 a protruding toward rotating cam 870. A movable valve element 821 is provided on main body 810 between rotating cam 870 and fixed valve element 811. At a position of movable valve element 821 opposite to fixed projection 811 a, a movable projection 821 b is provided.

At one end of movable valve element 821, a rotation shaft 821 a is provided, and movable valve element 821 is fixed on main body 810 rotatable about rotation shaft 821 a as the center. At the other end of movable valve element 821, a contact roller 831 rotatable about a rotation shaft 831 a and in contact with rotating cam 870 is provided.

A fixed valve element 812 is fixed on main body 810 on the left side of rotating cam 870. Fixed valve element 812 has a fixed projection 812 a protruding toward rotating cam 870. A movable valve element 822 is provided on main body 810 between rotating cam 870 and fixed valve element 812. At a position of movable valve element 822 opposite to fixed projection 812 a, a movable projection 822 b is provided.

At a lower end of movable valve element 822, a rotation shaft 822 a is provided, and movable valve element 822 is fixed on main body 810 rotatable about rotation shaft 822 a as the center. At the other end of movable valve element 822, a contact roller 841 rotatable about a rotation shaft 841 a and in contact with rotating cam 870 is provided.

Next, the states of operation of the second flow path switching device 800A will be described with reference to FIGS. 26 to 29. Though main tube 17 and branch tube 17 a are mounted on main body 810 fixed on cover 851, for convenience of description, cover 851 is not shown.

Referring to FIG. 26, rotating cam 870 is fixed at an initial state position. In this state, between fixed projection 811 a and movable projection 821 b, there is a space equal to or wider than the outer diameter of main tube 17. Similarly, between fixed projection 812 a and movable projection 822 b, there is a space equal to or wider than the outer diameter of branch tube 17 a.

Referring to FIG. 27, rotating cam 870 is rotated counterclockwise by 90°. Thus, contact roller 831 is pushed upward by the cam face of rotating cam 870. As a result, main tube 17 is pinched between fixed projection 811 a and movable projection 821 b, and the tube path of main tube 17 is closed. At this time, branch tube 17 a is open.

This state corresponds to the state where tube 22 and blood pressure transducer 300 are communicated in FIG. 7, and it is possible to measure blood pressure of the patient (blood pressure measuring state).

Referring to FIG. 28, rotating cam 870 is further rotated counterclockwise by 90°. Thus, while the state in which contact roller 831 is pushed upward by the cam face of rotating cam 870 is maintained, contact roller 841 is pushed to the left by the cam face of rotating cam 870. As a result, main tube is pinched between fixed projection 811 a and movable projection 821 b and tube path of main tube 17 is closed, and at the same time, branch tube 17 a is pinched between fixed projection 812 a and movable projection 822 b, and the tube path of branch tube 17 a is closed (closed state).

Referring to FIG. 29, rotating cam 870 is further rotated counterclockwise by 90°. Thus, pushing of contact roller 831 upward by the cam face of rotating cam 870 is cancelled, and main tube 17 is released. On the other hand, contact roller 841 is kept pushed to the left by the cam face of rotating cam 870, and tube path of main tube 17 is opened.

This state corresponds to the state in which tube 22 is communicated with injector head 1 with rotation mechanism in FIG. 7, and injection of contrast agent to the patient is possible (contrast agent injection state).

When rotating cam 870 is further rotated counterclockwise by 90°, the state of FIG. 26 is resumed. It is noted that for the switching between the blood pressure measuring state shown in FIG. 27 and the contrast agent injection state shown in FIG. 29, rotation of rotating cam 870 is controlled such that the closed state shown in FIG. 28 is interposed. The time required for rotation of rotating cam 870 for switching between the blood pressure measuring state and the contrast agent injecting state is about 0.3 seconds.

In injector head 1 with rotating mechanism in accordance with the present embodiment described above, the first and second syringes 510A and 510B are arranged along the up/down (vertical) direction with respect to injector head body 100 in the priming orientation and the contrast agent injectable orientation.

The state of mounting, however, is not limited to the above. By way of example, when viewed in the contrast agent injectable orientation corresponding to FIG. 4, the state of mounting in which syringes are arranged diagonally with respect to the rotation axis AL such as shown in FIG. 30, the state of mounting in which syringes are arranged side by side in horizontal direction as shown in FIG. 31 or other state of mounting may be adopted.

The embodiments as have been described here are mere examples and should not be interpreted as restrictive. The scope of the present invention is determined by each of the claims with appropriate consideration of the written description of the embodiments and embraces modifications within the meaning of, and equivalent to, the languages in the claims.

REFERENCE SIGNS LIST

1 injector head with rotation mechanism, 10A first tube, 10B second tube, 11A first T-shaped tube, 11B second T-shaped tube. 11C third T-shaped tube, 11D fourth T-shaped tube, 12 coupling tube, 13, 14, 20, 23, 24, 25, 26 connectors, 15 seventh tube, 15A eighth tube, 15B ninth tube, 16 contrast agent bag, 17 main tube, 17 a branch tube, 19 normal saline tube, 21 saline bag, 22 tube, 100 injector head body, 100 a first surface, 100 b second surface, 100 c third surface, 100 d fourth surface, 100P plunger, 100Pa first plunger, 100Pb second plunger, 110 operation monitor, 111A third tube, 111B fourth tube, 112A fifth tube, 112B sixth tube, 300 blood pressure transducer, 400 roller pump, 510A first syringe, 510B second syringe, 511 piston, 511A first piston, 511B second piston, 511 a piston rubber, 511 b piston core, 512 through hole, 513 flange, 514 cylindrical part, 600 first flow path switching device, 600A first flow path switching mechanism, 600B second flow path switching mechanism, 601 first fixed valve element, 602 second fixed valve element, 603 first change-over valve element, 604 third fixed valve element, 605 fourth fixed valve element, 606 second change-over valve element, 700 rotating part, 800, 800A second flow path switching devices, 801, 802 fixed valve elements, 803 change-over valve element, 810 main body, 811, 812 fixed valve elements, 811 a, 812 a fixed projections, 821, 822 movable valve elements, 821 a, 822 a, 831 a, 841 a rotation shafts, 821 b, 822 b movable projections, 831, 841 contact rollers, 851 cover, 851 a tube receiving recess, 861, 862 engaging pieces, 870 rotating cam, 900 supporting post, 1000 bed, 2000 patient, 3000 engineer, 4000 doctor, AL rotation axis, AS1 first air sensor, AS2 second air sensor, AS3 third air sensor. L1000 contrast agent injection line, S1 multi-use section, S2, S3 one-time use sections, SL central axis line, Z contrast agent. 

1. Using an injector head including a first plunger adapted to be movable forward and backward and a second plunger adapted to be movable forward and backward, said injector head being provided with a first syringe including a first piston detachably coupled to said first plunger and a second syringe including a second piston detachably coupled to said second plunger, said first syringe having a first through hole provided at a front end side, said second syringe having a second through hole provided at a front end side, and in a state where a first tube is coupled to said first through hole and a second tube is coupled to said second through hole, a priming method conducted when a contrast agent is introduced to said first syringe and a contrast agent is introduced to said second syringe by said injector head; wherein a first T-shaped tube is coupled to the other end of said first tube; said first T-shaped tube is coupled to one end of each of a third tube and a fifth tube; a second T-shaped tube is coupled to the other end of said second tube; said second T-shaped tube is coupled to one end of each of a fourth tube and a sixth tube; a third T-shaped tube is coupled to the other end of each of said third tube and said fourth tube; to said third T-shaped tube, a seventh tube having the other end coupled to a bag of said contrast agent is coupled; a fourth T-shaped tube is coupled to the other end of each of said fifth tube and said sixth tube; to said fourth T-shaped tube, a coupling tube having the other end coupled to a connector is coupled; a first flow path switching mechanism for switching opening/dosing of said third tube and said fifth tube arranged parallel to each other, and a second flow path switching mechanism for switching opening/dosing of said fourth tube and said sixth tube arranged parallel to each other are provided; said first flow path switching mechanism has a first change-over valve element arranged between said third tube and said fifth tube and movable in a direction intersecting a direction of extension of said third tube and said fifth tube; said first flow path switching mechanism has a first fixed valve element at a position opposite to said first change-over valve element with said third tube interposed, and a second fixed valve element at a position opposite to said first change-over valve element with said fifth tube interposed; said second flow path switching mechanism has a second change-over valve element arranged between said fourth tube and said sixth tube and movable in a direction intersecting a direction of extension of said fourth tube and said sixth tube; said second flow path switching mechanism has a third fixed valve element at a position opposite to said second change-over valve element with said fourth tube interposed, and a fourth fixed valve element at a position opposite to said second change-over valve element with said sixth tube interposed; said priming method comprising the steps of: a first step of tilting said injector head and thereby tilting said first syringe and said second syringe to have said first through hole positioned upper than said first piston and said second through hole positioned upper than said second piston; a second step, following the first step, of moving said first change-over valve element to the side of said first fixed valve element to close said third tube and moving said second change-over valve element to the side of said third fixed valve element to close said fourth tube and, in this state, moving said first piston in said first syringe to the foremost position to discharge air in said first syringe to the outside and moving said second piston in said second syringe to the foremost position to discharge air in said second syringe to the outside; a third step, following the second step, of moving said second change-over valve element of said second flow path switching mechanism to the side of said fourth fixed valve element to open said fourth tube and to close said sixth tube and, in this state, with a contrast agent bag containing said contrast agent coupled to said second tube, moving said second piston in said second syringe backward to introduce a prescribed amount of said contrast agent from said contrast agent bag to said second syringe; a fourth step, following the third step, of moving said second change-over valve element to the side of said third fixed valve element to close said fourth tube and moving said first change-over valve element to the side of said second fixed valve element to close said fifth tube and, in this state, moving said second piston in said second syringe backward to introduce a prescribed amount of air to said second syringe; a fifth step, following the fourth step, of moving said first change-over valve element to the side of said first fixed valve element to close said third tube and, in this state, moving said second piston in said second syringe forward to discharge air in said second syringe to the outside and filling said second tube with said contrast agent; a sixth step, following the fifth step, of moving said first change-over valve element of said first flow path switching mechanism to the side of said second fixed valve element to open said third tube and to close said fifth tube and, in this state, moving said first piston in said first syringe backward to introduce a prescribed amount of said contrast agent from said contrast agent bag to said first syringe; a seventh step, following the sixth step, of moving said first change-over valve element to the side of said first fixed valve element to close said third tube and, in this state, moving said second piston in said second syringe backward to introduce a prescribed amount of air to said second syringe; and an eighth step, following the seventh step, of moving said second change-over valve element to the side of said fourth fixed valve element to close said sixth tube, and in this state, moving said second piston in said second syringe backward to introduce said contrast agent to said second syringe and, with said first tube being kept open, moving said second piston in said second syringe forward to discharge air in said second syringe to the outside and filling said first tube with said contrast agent.
 2. The priming method according to claim 1, wherein said coupling tube is further provided with a first air sensor for detecting entrance of air to said coupling tube; said seventh tube is further provided with a second air sensor for detecting entrance of air to said seventh tube; at said fifth step, said second piston in said second syringe is moved forward until passage of said contrast agent is detected by said first air sensor; and at said eighth step, said first piston in said first syringe is moved forward until passage of said contrast agent is detected by said first air sensor, and said second piston in said second syringe is moved backward until passage of said contrast agent is no longer detected by said second air sensor.
 3. The priming method according to claim 1, wherein said injector head includes a supporting part, a rotating part fixed on said supporting part to have a rotation axis extending substantially horizontally, an injector head body fixed on said rotating part to be rotatable about said rotation axis, and a syringe detachably attached to said injector head body; in a state where said first syringe and said second syringe are attached to said injector head body, when viewed from the direction perpendicular to and parallel to the rotation axis, central axis line of said first syringe and said second syringe is inclined with respect to said rotation axis; and by rotating said injector head body about said rotation axis as the center of rotation, selection is possible between a state in which said first syringe and said second syringe assume a priming orientation with said first through hole side of said first syringe and said second through hole side of said second syringe positioned upper than said injector head body and a state in which said first through hole of said first syringe assumes a contrast agent injectable orientation with said first through hole side of said first syringe and said second through hole of said second syringe positioned lower.
 4. The priming method according to claim 3, wherein said first through hole is provided at a position eccentric to said central axis line of said first syringe; said second through hole is provided at a position eccentric to said central axis line of said second syringe; said first syringe and said second syringe are attached to said injector head body such that when said first syringe and said second syringe are in said priming orientation, said first through hole and said second through hole are positioned at the uppermost positions. 